HEALTHCAREFull-time
Clinical Data Analyst III
By Admin · Clinical Data Management
BANGALORE (IN)REMOTEPOSTED: 9/10/2026
HEALTHCAREFull-time
HIRING ORGANIZATIONPAREXELBiosciences / Healthcare, Contract Research Organization (CRO)
ROLE OVERVIEW
Lead clinical data validation and data management activities across clinical studies, serving as a subject matter expert while ensuring data quality, regulatory compliance and successful database delivery.
ROLE DEFINITION & RESPONSIBILITIES
- •Independently lead clinical data validation, cleaning, review and reconciliation throughout study conduct and database lock
- •Manage data queries and manual and SAS-generated listing reviews
- •Reconcile external vendor data and maintain data integrity across systems
- •Identify project risks and support mitigation planning
- •Prepare and maintain Data Management documentation and Trial Master File records
- •Lead User Acceptance Testing activities for clinical database setups
- •Review protocols, EDC screens and database configurations
- •Coordinate study start-up activities, mentor analysts and support continuous improvement initiatives
Reporting Hierarchy: Reports to Data Management leadership and collaborates with sponsors, stakeholders and global clinical data management teams; provides mentoring and serves as SME for data management tools and processes
* Role responsibilities and qualifications synthesized based on industry benchmark standards.
QUALIFICATIONS & REQUIREMENTS
REQUIRED QUALIFICATIONS
- Bachelor's degree in Life Sciences, Pharmacy, Biotechnology, Nursing or related healthcare discipline
- Relevant Clinical Data Management experience within clinical research or CRO industry
- Strong experience with clinical data management systems
- Advanced knowledge of data cleaning, reconciliation and database lock activities
- Knowledge of ICH-GCP, clinical research regulations and industry best practices
- Experience leading virtual data management teams
PREFERRED QUALIFICATIONS
- •Experience with Medidata Rave, Oracle InForm, Veeva, DataLabs or ClinBase
- •Knowledge of MedDRA and WHODrug
- •Understanding of CDISC standards
- •Basic knowledge of SAS and programmed listings
REQUIRED VERIFIED SKILLS
Clinical Data Management
Clinical Data Validation
Data Cleaning
Data Reconciliation
Database Lock
EDC
Medidata Rave
Oracle InForm
Veeva
DataLabs
ClinBase
ICH-GCP
Regulatory Compliance
UAT
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
Benefits: Professional development, mentoring and training opportunities; global clinical research environment; employee-focused culture
No salary or bonus/equity figures are disclosed in the supplied posting. Compensation should be confirmed directly with Parexel during the recruitment process.
ORGANIZATION CONTEXT & CULTURE
Parexel is a global clinical research organization providing clinical development solutions spanning clinical trials, regulatory, consulting and market access, with a mission focused on improving global health.
TEAM SIZE: 20,000+ employees
INDUSTRY: Biosciences / Healthcare, Contract Research Organization (CRO)
Culture: Parexel emphasizes empathy, collaboration, quality and meaningful contribution to the development of therapies that benefit patients.
EXPECTED CAREER ROADMAP
Can progress toward Senior Clinical Data Management roles, Data Management Lead, Clinical Data Management Project leadership, SME or broader clinical operations management positions.
APPLICATION ADVISORY
Emphasize clinical data management leadership, EDC expertise, database lock and reconciliation experience; highlight Medidata Rave or comparable systems; demonstrate ICH-GCP knowledge, sponsor interaction, risk management and mentoring experience; quantify process improvements or quality outcomes where possible.
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
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